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      Progress and Perspectives of Electrochemical CO2 Reduction on Copper in Aqueous Electrolyte

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          Abstract

          <p class="first" id="d1606359e196">To date, copper is the only heterogeneous catalyst that has shown a propensity to produce valuable hydrocarbons and alcohols, such as ethylene and ethanol, from electrochemical CO2 reduction (CO2R). There are variety of factors that impact CO2R activity and selectivity, including the catalyst surface structure, morphology, composition, the choice of electrolyte ions and pH, and the electrochemical cell design. Many of these factors are often intertwined, which can complicate catalyst discovery and design efforts. Here we take a broad and historical view of these different aspects and their complex interplay in CO2R catalysis on Cu, with the purpose of providing new insights, critical evaluations, and guidance to the field with regard to research directions and best practices. First, we describe the various experimental probes and complementary theoretical methods that have been used to discern the mechanisms by which products are formed, and next we present our current understanding of the complex reaction networks for CO2R on Cu. We then analyze two key methods that have been used in attempts to alter the activity and selectivity of Cu: nanostructuring and the formation of bimetallic electrodes. Finally, we offer some perspectives on the future outlook for electrochemical CO2R. </p>

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          Author and article information

          Journal
          Chemical Reviews
          Chem. Rev.
          American Chemical Society (ACS)
          0009-2665
          1520-6890
          May 22 2019
          May 22 2019
          Affiliations
          [1 ]SUNCAT Center for Interface Science and Catalysis, Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States
          [2 ]Section for Surface Physics and Catalysis, Department of Physics, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark
          [3 ]Institute of Surface Chemistry and Catalysis, Ulm University, D-89069 Ulm, Germany
          [4 ]Department of Materials, Imperial College London, Royal School of Mines, London SW7 2AZ, United Kingdom
          [5 ]SUNCAT Center for Interface Science and Catalysis, SLAC National Accelerator Laboratory, Menlo Park, California 94025, United States
          Article
          10.1021/acs.chemrev.8b00705
          31117420
          e75ae222-32d6-474d-b063-f45aa7435704
          © 2019
          History

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